Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/16—Nitrogen-containing compounds
  • C08K5/34—Heterocyclic compounds having nitrogen in the ring
  • C08K5/35—Heterocyclic compounds having nitrogen in the ring having also oxygen in the ring
  • C08K5/357—Six-membered rings
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
  • C08G59/02—Polycondensates containing more than one epoxy group per molecule
  • C08G59/04—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof
  • C08G59/06—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols
  • C08G59/066—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols with chain extension or advancing agents
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
  • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
  • C08G59/68—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the catalysts used
  • C08G59/686—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the catalysts used containing nitrogen
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
  • C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
  • C08L2666/14—Macromolecular compounds according to C08L59/00 - C08L87/00; Derivatives thereof
  • C08L2666/22—Macromolecular compounds not provided for in C08L2666/16 - C08L2666/20
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
  • Y10T428/2913—Rod, strand, filament or fiber
  • Y10T428/2933—Coated or with bond, impregnation or core

Definitions

• the present invention relates to a polymerizable composition containing at least one benzoxazine compound and certain oligomeric or polymeric urethane group-free polyether compounds.
• the present invention also relates to adhesives, sealants or coatings comprising the polymerizable composition according to the invention, and to polymerization products of said composition.
• Epoxide-based resin systems have long been successfully used in the aviation, automotive and electronics industry as adhesives, sealants or as surface coatings or used as resin systems with a range of different materials for producing composite materials.
• Benzoxazine-based resin systems generally have a high glass transition temperature and high mechanical strength. Furthermore the cited materials are distinguished by their good electrical properties and their positive fire protection behavior.
• benzoxazine-based resin systems lie in their fracture-mechanical properties. The materials are often very brittle after they have cured, and for most applications they have to be impact-modified by the addition of toughening agents.
• the International patent application WO 2007/064801 teaches a curable composition comprising benzoxazine-based resin systems and certain adducts as toughening agents.
• the cited adducts are produced in two steps. In a first step a first compound containing hydroxyl groups is reacted with a compound containing isocyanate groups and a phenolic compound to form a reaction product containing urethane groups. In a second step the urethane group-containing reaction product is reacted further with epoxide-containing compounds to obtain the aforementioned adducts as toughening agents.
• the toughening agent production process disclosed in WO 2007/064801 can be regarded as being capable of improvement from both a cost and an efficiency perspective. Furthermore, owing to environmental considerations it is desirable to avoid the use of isocyanates in the production of toughening agents.
• the object of the present invention was therefore to provide a benzoxazine-based polymerizable composition containing at least one toughening agent that can be produced in a simple and cost-effective method from readily available raw materials without the use of isocyanates, wherein in its cured state the polymerizable composition has improved fracture-mechanical properties as compared with the prior art.
• polymerizable compositions containing at least one benzoxazine compound can be impact-modified in an effective manner by the addition of certain oligomeric or polymeric urethane group-free polyether compounds as toughening agents, as a result of which in their cured form the polymerizable compositions have very good fracture-mechanical properties.
• the present invention thus firstly provides a polymerizable composition comprising
• each residue R a in each repeating unit independently denotes a divalent group of compounds comprising 1 to 100 C atoms
• each residue X′ in each repeating unit is independently selected from —O—, —S—, —NH— or a carboxyl group of the general form —(C ⁇ O)O—, in which the C atom of the carboxyl group is always connected to the residue A
• each residue Y in each repeating unit is independently selected from —OH, —SH and —NH 2
• each residue A in each repeating unit is independently selected from K or L
• L denoting a divalent residue of polyethers following removal of two terminal hydroxyl groups
• the present invention also provides a polymerizable composition comprising
• each residue R d and R e independently denotes a divalent group of compounds comprising 1 to 100 C atoms
• each residue X′ is independently selected from —O—, —S—, —NH— or a carboxyl group of the general form —(C ⁇ O)O—, in which the C atom of the carboxyl group is always connected to the residue D
• W is selected from —O—, —S— or —NH— and the residue D comprises at least one aromatic group, with the proviso that the exclusive reaction of one or more component(s) satisfying the definition of (A-1) with one or more component(s) satisfying the definition of (B-2) and the exclusive reaction of one or more component(s) satisfying the definition of (A-2) with one or more component(s) satisfying the definition of (B-1) is excluded.
• the polymerizable compositions of the present invention are exceptionally suitable for producing adhesives, sealants or coating agents and for producing composite materials comprising a layer or a bundle of fibers, such as carbon fibers for example.
• the present invention therefore also provides adhesives, sealants or coating agents comprising the polymerizable composition according to the invention and the polymerization product of the composition according to the invention, wherein said polymerization product can be in contact with a layer or a bundle of fibers, such as carbon fibers for example.
• the present invention also provides the use of one or more of the aforementioned oligomeric or polymeric urethane group-free polyether compounds as impact modifiers for a polymerization product containing at least one polymerizable benzoxazine compound in polymerized form.
• the benzoxazine compound of the present invention is a monomer, oligomer or polymer comprising at least one benzoxazine group.
• Preferred monomers can preferably comprise up to four benzoxazine groups, wherein both individual monomers and mixtures of two or more monomers can be used as the benzoxazine compound.
• Suitable benzoxazine compounds are preferably described by formula (B-I),
• R 1 is selected from the group consisting of hydrogen, alkyl, alkenyl and aryl
• R 4 is selected from the group consisting of hydrogen, halogen, alkyl and alkenyl
• R 4 is a divalent residue that makes a corresponding naphthoxazine structure from the benzoxazine structure.
• R 1 and R 2 are identical or different and are each selected from the group consisting of hydrogen, alkyl, in particular methyl, ethyl, n-propyl, i-propyl, n-butyl or i-butyl, alkenyl, in particular allyl, and aryl, and the substituents R 4 are identical or different and are each selected from the group consisting of hydrogen, halogen, alkyl and alkenyl, or R 4 is a divalent residue that makes a corresponding naphthoxazine structure from the benzoxazine structure.
• Preferred benzoxazine compounds according to formula (B-II) are for example benzoxazine compounds according to formula (B-III) to (B-VI),
• R 1 , R 2 and R 4 are as defined in formula (B-I) and/or (B-II).
• Preferred benzoxazine compounds are moreover compounds of the general formula (B-VII),
• R 4 is selected from the group consisting of hydrogen, halogen, alkyl and alkenyl, or R 4 is a divalent residue that makes a corresponding naphthoxazine structure from the benzoxazine structure.
• benzoxazine compounds are moreover compounds of the general formula (B-VIII) to (B-X),
• R 1 , R 2 and R 4 are as defined in formula (B-I) and/or (B-II) and R 3 is defined in the same way as R 1 or R 2 .
• Suitable benzoxazine compounds within the meaning of the present invention are for example the following compounds:
• a further benzoxazine compound that can be used within the context of the present invention is selected from compounds of the formula (B-XIX),
• each R in formula (XIX) is independently selected from allyl, aryl, C 1 -C 8 alkyl and C 3 -C 8 cycloalkyl.
• the aforementioned groups can be in substituted or unsubstituted form, suitable substituents being selected for example from amino, allyl and C 1 -C 8 alkyl.
• Suitable benzoxazine compounds within the meaning of the present invention are both monofunctional and polyfunctional benzoxazine compounds.
• Monofunctional benzoxazine compounds are understood to be compounds comprising only one benzoxazine group, whereas polyfunctional benzoxazine compounds comprise more than one benzoxazine group and can preferably contain up to four benzoxazine groups.
• Monofunctional benzoxazine compounds can be described by way of example by the general formula (XIX),
• R in formula (B-XIX) is selected from the group consisting of alkyl, in particular methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, alkenyl, in particular allyl, and aryl, wherein each of the cited groups is optionally substituted and R 4 is selected from the group consisting of hydrogen, halogen, alkyl and alkenyl, or R 4 is a divalent residue that makes a corresponding naphthoxazine structure from the benzoxazine structure.
• Preferred monofunctional benzoxazine compounds are described for example by the general formula (B-XX),
• R I is selected from the group consisting of alkyl and alkenyl, wherein each of the cited residues is optionally substituted or interrupted by one or more O, N, S, C ⁇ O, COO or NHC ⁇ O or by one or more aryl groups
• m is an integer number between 0 and 4
• R II , R III , R IV , R V and R VI are selected independently of each other from the group consisting of hydrogen, alkyl and alkenyl, wherein each alkyl or alkenyl group is optionally substituted or interrupted by one or more O, N, S, C ⁇ O, COO or NHC ⁇ O or by one or more aryl groups.
• Suitable monofunctional benzoxazine compounds within the meaning of the present invention are for example the following compounds (B-XXI) and (B-XXII),
• R I is defined as in formula (B-XX).
• Benzoxazine compounds within the meaning of the present invention are commercially available and are sold inter alia by Huntsman Advanced Materials; Georgia-Pacific Resins, Inc. and Shikoku Chemicals Corporation, Chiba, Japan.
• the benzoxazine compounds according to the invention of the present invention can also be obtained by reacting a phenolic compound, for example bisphenol A, bisphenol F, bisphenol S or thiophenol, with an aldehyde, for example formaldehyde, in the presence of a primary alkylamine or arylamine.
• a phenolic compound for example bisphenol A, bisphenol F, bisphenol S or thiophenol
• an aldehyde for example formaldehyde
• Suitable production methods are disclosed for example in U.S. Pat. No. 5,543,516, in particular in examples 1 to 19 in columns 10 to 14, wherein the reaction time for the corresponding reaction can last from a few minutes to a few hours, depending on the concentration, reactivity and reaction temperature.
• Further production possibilities for the benzoxazine compounds according to the invention can be obtained from U.S. Pat. Nos. 4,607,091, 5,021,484 and 5,200,452 and from the International patent application WO 2006/0350
• the polymerizable composition contains at least one polymerizable benzoxazine compound or a mixture of various polymerizable benzoxazine compounds in amounts from 20 to 90 wt. %, preferably from 30 to 80 wt. % and extremely preferably from 50 to 70 wt. %, relative in each case to the total amount of the preparation.
• the polymerizable composition according to the invention moreover comprises at least one of the aforementioned oligomeric or polymeric urethane group-free polyether compounds.
• a “polyether compound” within the meaning of the present invention is understood to refer to compounds containing four or more than four ether linkages.
• Oligomeric polyether compounds contain 4 to 20 ether linkages, while polymeric polyether compounds comprise more than 20 ether linkages.
• urethane group-free polyether compound is understood to refer to oligomeric or polymeric polyether compounds whose polymer chains are substantially free from urethane groups (—NH—CO—O—). “Substantially free” means that the proportion of urethane groups relative to the molecular weight of a molecule of the oligomeric or polymeric polyether compound is less than 0.5%, preferably less than 0.25% and particularly preferably less than 0.1%.
• the oligomeric or polymeric polyether compound is completely free from urethane groups, such that the proportion of urethane groups relative to the molecular weight of each molecule of the oligomeric or polymeric polyether compound is 0%.
• Urethane groups in a polymer chain are generally formed by the reaction of an alcohol with an isocyanate.
• the urethane group-free polyether compounds as impact modifiers, the use of isocyanate-containing compounds can substantially be dispensed with in their production.
• the polymerizable compositions according to the invention containing urethane group-free polyether compounds as toughening agents have a markedly reduced viscosity as compared with comparable compositions having urethane group-containing polyether compounds.
• the viscosity of the polymerizable compositions according to the invention thus remains low, even if relatively large amounts of urethane group-free polyether compounds are used as impact modifiers.
• the oligomeric or polymeric urethane group-free polyether compound of the present invention has at least one terminal hydroxyl, carboxyl, amino or thiol group, preferably at least one terminal hydroxyl group, and/or at least one terminal oxirane, aziridine or thiirane group, preferably at least one terminal oxirane group.
• All terminal groups of the oligomeric or polymeric urethane group-free polyether compound of the present invention are selected in particular from hydroxyl, carboxyl, amino, thiol, oxirane, aziridine and/or thiirane groups, particularly preferably from hydroxyl and/or oxirane groups.
• the terminal groups can react with the benzoxazine compound to form a covalent bond, resulting in a particularly effective binding of the toughening agent to the resin matrix.
• An improved impact modification of the cured polymerizable composition according to the invention is achieved in this way.
• Preferred oligomeric or polymeric urethane group-free polyether compounds have a weight-average molecular weight from 1000 to 100,000 g/mol, preferably from 2000 to 8000 g/mol and particularly preferably from 3000 to 5000 g/mol.
• Oligomeric or polymeric urethane group-free polyether compounds having a weight-average molecular weight below 1000 g/mol can act in the resin matrix as a plasticizer, causing polymerization products to be obtained that because of their fracture-mechanical properties and their comparatively low flexural moduli are unsuitable for most application purposes, in particular in composite materials.
• Oligomeric or polymeric urethane group-free polyether compounds having a weight-average molecular weight above 100,000 g/mol generally have a very high viscosity. It is therefore possible for the aforementioned polyether compounds to exhibit a comparatively poor compatibility with the resin matrix.
• the oligomeric or polymeric urethane group-free polyether compound of the present invention comprises one or more structural elements of the general formula (I),
• each residue R a in each repeating unit independently denotes a divalent group of compounds comprising 1 to 100 C atoms
• each residue X′ in each repeating unit is independently selected from —O—, —S—, —NH— or a carboxyl group of the general form —(C ⁇ O)O—, in which the C atom of the carboxyl group is always connected to the residue A
• each residue Y in each repeating unit is independently selected from —OH, —SH and —NH 2
• each residue A in each repeating unit is independently selected from K or L
• L denoting a divalent residue of polyethers following removal of two terminal hydroxyl groups
• Divalent residue K is formally obtained by removing two hydroxyl groups from aromatic dihydroxyl compounds.
• aromatic dihydroxyl compounds are understood to be all compounds comprises two hydroxyl groups, each hydroxyl group being covalently bonded to a C atom of an aromatic or heteroaromatic ring system.
• the two hydroxyl groups can be bonded either to the same or to two different aromatic or heteroaromatic ring systems.
• Divalent residue L is formally obtained by removing two terminal hydroxyl groups from polyethers. Residue L thus comprises all divalent groups having the aforementioned chemical structure. It is obvious that the chemical structure of residue L can formally also be obtained in many other ways, for example by removing two terminal amino groups from amino-terminated polyethers. Such residues too naturally fall within the above definition of residue L.
• Divalent residue L is preferably formally obtained by removing two terminal hydroxyl groups from “non-aromatic polyethers”, wherein within the meaning of the present invention the term “non-aromatic polyethers” is understood to mean polyethers comprising no aromatic structural element.
• divalent residue L is formally obtained by removing two terminal hydroxyl groups from polyalkylene oxides, non-aromatic polyalkylene oxides being particularly preferred.
• oligomeric or polymeric urethane group-free polyether compounds that comprise structural elements derived from non-aromatic polyethers and/or polyalkylene oxides as residue L exhibit a particularly good action as impact modifiers.
• the oligomeric or polymeric urethane group-free polyether compound comprises a plurality of structural elements of the general formula (I)
• the cited structural elements can be identical or different and can be connected to one another by one or more groups of compounds of any kind.
• the individual group of compounds are identical or different and are preferably selected from covalent bonds and linear or branched di-, tri-, tetra-, penta- or polyvalent groups each comprising 1 to 100 C atoms.
• the aforementioned groups of compounds are preferably selected from C 1-22 alkyls, in particular C 6-22 alkyls, C 2-22 alkenyls, in particular C 6-22 alkenyls, C 2-22 alkynyls, in particular C 6-22 alkynyls, C 6-8 cycloalkyls, C 3-22 heteroalkyls, C 4-22 heterocycloalkyls, C 6-14 aryls and C 6-14 heteroaryls.
• All aforementioned groups of compounds can independently of one another each be substituted one or more times, in particular one, two or three times, preferably once, in particular by substituents selected from halogen, in particular chlorine, bromine or fluorine, trifluoromethyl, C 1-18 alkyl, C 3-8 cycloalkyl, C 2-18 alkenyl, C 2-18 alkynyl, heteroalkyl, heterocycloalkyl, C 1-18 alkoxy, C 1-18 alkylsulfanyl, C 1-18 alkylsulfonyl, C 1-18 alkylsulfoxidyl, C 1-18 alkanoyl, C 1-18 alkanoyloxy, C 1-18 alkoxycarbonyl, C 1-18 alkylaminocarbonyl, C 1-18 alkylsulfanylcarbonyl, sulfanyl, cyano, amino, heteroaryl, heteroaryl(C 1-12 alkyl), heteroaryloxy, heteroarylamino, heteroarylsul
• the proportion of residue K relative to the total number of all residues A in the oligomeric or polymeric urethane group-free polyether compound is 30 to 70%, preferably 40 to 60% and in particular 45 to 55%.
• Oligomeric or polymeric urethane group-free polyether compounds containing the aforementioned proportions of residues K exhibit particularly good compatibility with the benzoxazine resin matrix.
• the proportion of residue L relative to the total number of all residues A in the oligomeric or polymeric urethane group-free polyether compound is 30 to 70%, preferably 40 to 60% and in particular 45 to 55%.
• Oligomeric or polymeric urethane group-free polyether compounds containing the aforementioned proportion of residues L have a comparatively lower glass transition temperature T g and a reduced viscosity, giving rise to polymerizable compositions having particularly good processability.
• the compatibility, viscosity and glass transition temperature of the oligomeric or polymeric urethane group-free polyether compound can be precisely adjusted by means of the appropriate choice of the percentages of residues K and L.
• the impact strength, flexural properties and post-cure microstructure of the polymerization products according to the invention can be selectively controlled by means of the percentage ratios of residues K and L in the oligomeric or polymeric urethane group-free polyether compound as a function of the benzoxazine compound or mixture of various benzoxazine compounds used.
• oligomeric or polymeric urethane group-free polyether compounds are preferred in particular in which the proportion of all structural elements of formula (I) relative to the weight-average molecular weight of the oligomeric or polymeric urethane group-free polyether compound is 40 to 99.99%, preferably 70 to 99% and in particular 85 to 98%.
• Oligomeric or polymeric urethane group-free polyether compounds containing the aforementioned proportions of structural elements of formula (I) make it possible to achieve a particularly effective impact modification of the cured polymerizable compositions according to the invention.
• the individual structural elements of the general formula (I) can be aligned or linked together in such a way that they form a linear oligomeric or polymeric urethane group-free polyether compound of the present invention and/or are a constituent of such a compound.
• the individual structural elements of the general formula (I) can be aligned or linked together in such a way that they form a branched oligomeric or polymeric urethane group-free polyether compound of the present invention and/or are a constituent of such a compound.
• preferred oligomeric or polymeric urethane group-free polyether compounds are selected from compounds of the general formula (II),
• F is selected from hydrogen or residues of the general formula (IV),
• each residue W in formula (III) and (IV) is independently selected from —O—, —S— or —NH—, in which W denotes in particular —O—, n is a number from 5 to 10,000
• each residue R a in each repeating unit and in formula (II) independently denotes a divalent group of compounds comprising 1 to 100 C atoms
• each residue X′ in each repeating unit and in formula (II) and (IV) is independently selected from —O—, —S—, —NH— or a carboxyl group of the general form —(C ⁇ O)O—, in which the C atom of the carboxyl group is always connected to the residue A
• each residue Y in each repeating unit and in formula (IV) is independently selected from —OH, —SH and —NH 2 and each residue A in each repeating unit and in formula (IV) is independently selected from K or L, K denoting a divalent residue of aromatic dihydroxyl compounds following removal of both
• n in formula (I) and (II) preferably denotes a number from 3 to 20, particularly preferably a number from 5 to 15 and extremely preferably a number from 7 to 10.
• each residue R a in formula (I), (II), (III) and/or (IV) is independently selected from alkylene groups containing 1 to 10 C atoms.
• R a is selected from linear alkylene groups comprising 1 to 6, in particular 1 or 2 carbon atoms, such as for example methylene and ethylene groups, R a particularly preferably denoting a methylene group in the aforementioned formulae.
• each residue X′ in formula (I), (II) and/or (IV) independently denotes —O—.
• This can be achieved in particular by using aromatic substances having at least two aromatic hydroxyl groups and/or polyethers having at least two terminal hydroxyl groups in the production of the urethane group-free polyether compounds of the present invention.
• aromatic substances having at least two aromatic hydroxyl groups and/or polyethers having at least two terminal hydroxyl groups in the production of the urethane group-free polyether compounds of the present invention.
• the use of the aforementioned substances is advantageous because they can be produced cost-effectively or are commercially available in a wide variety of structures.
• residue Y in formula (I), (II) and/or (IV) is furthermore preferable for residue Y in formula (I), (II) and/or (IV) to denote —OH.
• residue Y in formula (I), (II) and/or (IV) can be achieved in particular by using substances having terminal oxirane groups in the production of the urethane group-free polyether compounds of the present invention.
• the use of the aforementioned substances is advantageous because they can be produced cost-effectively and are commercially available in a wide variety of structures.
• Divalent residue K is formally obtained by removing two hydroxyl groups from aromatic dihydroxyl compounds.
• Preferred residues K in each repeating unit and in each of the formulae (I), (II) and optionally (IV) are selected independently of one another from divalent residues of the general formula (V) and/or formula (VI),
• Q is selected from alkylene, oxygen, sulfur, sulfoxide, sulfone and a direct, covalent bond and i and j independently of each other denote a number from 0 to 4, in particular 0 or 1.
• residues R b and R c are selected independently of one another from halogen, in particular fluorine, chlorine, bromine or iodine, C 1-40 alkyl, for instance methyl, ethyl, isopropyl, C 2-40 alkenyl, C 1-40 alkoxyl and C 7-13 aralkyl.
• Residue R b in formula (V) can also be a divalent residue that makes a corresponding naphthyl group from the phenyl group.
• residues R b and R c if present, comprise at least one further structural element of the general formula (I).
• alkylene group Q is understood to refer to divalent alkyl residues, i.e. alkyls that can still bond on both sides.
• Preferred alkylene residues are for example substituted or unsubstituted, saturated or unsaturated alkylene residues having 1 to 40 C atoms.
• Preferred compounds are selected from for example —CH 2 — (methylene), —CH 2 —CH 2 — (ethylene), —CH 2 —CH 2 —CH 2 -(propylene), —CH 2 —CH 2 —CH 2 —CH 2 — (butylene), —CH 2 —CH 2 —CH 2 —CH 2 — (hexylene), —CH 2 —CH 2 —CH 2 —CH 2 —CH 2 — (heptylene), —CH 2 —CH 2 —CH 2 —CH 2 —CH 2 —CH 2 —CH 2 —CH 2 —CH 2 -(octylene), but also from the branched derivatives thereof, such as isopropylene, tert-butylene.
• the alkylene group Q can be mono- or polysubstituted. Suitable substituents can be selected for example from halogen, in particular chlorine, bromine or fluorine, trifluoromethyl, C 1-18 alkyl, C 3-8 cycloalkyl, C 2-18 alkenyl, C 2-18 alkynyl, heteroalkyl, heterocycloalkyl, C 1-18 alkoxy, C 1-18 alkylsulfanyl, C 1-18 alkylsulfonyl, C 1-18 alkylsulfoxidyl, C 1-18 alkanoyl, C 1-18 alkanoyloxy, C 1-18 alkoxycarbonyl, C 1-18 alkylaminocarbonyl, C 1-18 alkylsulfanylcarbonyl, sulfanyl, cyano, amino, heteroaryl, heteroaryl(C 1-12 alkyl), heteroaryloxy, heteroarylamino, heteroarylsulfanyl, heteroarylsulfonyl
• naphthalene diols such as for instance 1,2-naphthalene diol, 2,6-naphthalene diol, 2,7-naphthalene diol, bis-(4-hydroxyphenyl), 2,2-bis-(4-hydroxyphenyl)propane, bis-(4-hydroxyphenyl)sulfide, bis-(4-hydroxyphenyl)ether, bis-(4-hydroxyphenyl)ketone, bis-(4-hydroxyphenyl)sulfone, bis-(4-hydroxyphenyl)methane, 1,1-bis-(4-hydroxyphenyl)cyclohexane, ⁇ , ⁇ ′-bis-(4-hydroxyphenyl)-p-diisopropylbenzene, 1,1-bis-(4-hydroxyphenyl)-1-phenylethane, 2,2-bis-(3-methyl-4-hydroxyphenyl)propane, 2,2-bis-(3,5-dichloro-4-hydroxy
• Divalent residue L is formally obtained by removing two terminal hydroxyl groups from polyethers.
• Preferred residues L in each repeating unit and in each of the formulae (I), (II) and optionally (IV) are selected independently of one another from divalent residues of the general formula (VII),
• each I′ in formula (VII) and in each repeating unit independently denotes a number from 1 to 10
• each R in formula (VII) and in each repeating unit is independently selected from hydrogen or linear or branched optionally substituted C 1-12 alkyl groups, R denoting hydrogen or methyl in particular.
• I denotes a number from 1 to 200, preferably a number from 3 to 50 and particularly preferably a number from 5 to 20 and/or I′ in formula (VII) and in each repeating unit independently denotes 1, 2, 3, 4, 5, 6, 7 or 8, in particular 1 or 3.
• each residue L has a weight-average molecular weight (M w ) from 200 to 10,000 g/mol, preferably from 300 to 5000 g/mol and in particular from 500 to 2000 g/mol, prior to removal of two terminal hydroxyl groups. It is furthermore advantageous for each residue L to have a glass transition temperature (T g ) of less than 20° C., preferably less than 10° C. and particularly preferably less than 0° C., prior to removal of two terminal hydroxyl groups.
• M w weight-average molecular weight
• T g glass transition temperature
• the weight-average molecular weight (M w ) is determined by gel permeation chromatography (GPC) using polystyrene as the standard.
• the glass transition temperature (T g ) is determined by dynamic mechanical thermal analysis (DMTA), the individual glass transition temperature being obtained from the maximum value of the graph plotting loss modulus against temperature.
• the oligomeric or polymeric urethane group-free polyether compound of the present invention is obtainable by reacting at least one component A with at least one component B, component A being selected from the group consisting of
• A-2 polyethers having at least two terminal hydroxyl, carboxyl, amino or thiol groups, and component B being selected from the group consisting of
• each residue R d and R e independently denotes a divalent group of compounds comprising 1 to 100 C atoms
• each residue X′ is independently selected from —O—, —S—, —NH— or a carboxyl group of the general form —(C ⁇ O)O—, in which the C atom of the carboxyl group is always connected to the residue D
• W is selected from —O—, —S— or —NH— and the residue D comprises at least one aromatic group, with the proviso that the exclusive reaction of one or more component(s) satisfying the definition of (A-1) with one or more component(s) satisfying the definition of (B-2) and the exclusive reaction of one or more component(s) satisfying the definition of (A-2) with one or more component(s) satisfying the definition of (B-1) is excluded.
• oligomeric or polymeric urethane group-free polyether compound one or more component(s) A is/are reacted with one or more component(s) B, each component used having a different chemical structure.
• exclusive reaction is understood to mean that the reaction of two components takes place without at least one component being present in the reaction that satisfies none of the definitions of the aforementioned components.
• reaction of one or more components satisfying the definition of (A-1) with one or more components satisfying the definition of (B-2) is excluded only in the case where no component is present in the reaction that does not satisfy the definition of (A-1) and (B-2).
• reaction of one or more components satisfying the definition of (A-2) with one or more components satisfying the definition of (B-1) is excluded only in the case where no component is present in the reaction that does not satisfy the definition of (A-2) and (B-1).
• hydroxyl, carboxyl, amino and/or thiol groups of one component react in particular with terminal oxirane, aziridine or thiirane groups of another component to form an oligomeric or polymeric urethane group-free polyether compound.
• the reaction described preferably takes place at temperatures from 20 to 250° C., for instance at 100° C. to 180° C.
• the reaction time is likewise dependent on the reactivity of the components used and is preferably 10 min to 12 h, in particular 1 h to 6 h, wherein the reaction can be performed in a suitable solvent, such as for example toluene, or without solvent.
• Suitable catalysts accelerate the reaction of hydroxyl, carboxyl, amino and/or thiol groups with terminal oxirane, aziridine or thiirane groups and are selected in particular from tetraalkyl ammonium salts, such as for example tetrabutyl ammonium bromide, tertiary amines, such as for example 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), aryl/alkyl phosphines, such as for example triphenylphosphine, or ureas, such as for example Versamine EH-50.
• tetraalkyl ammonium salts such as for example tetrabutyl ammonium bromide
• tertiary amines such as for example 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU)
• aryl/alkyl phosphines such as for example triphenylphosphin
• the reaction of the individual components is performed in the presence of at least one crosslinking agent.
• Suitable crosslinking agents can be selected for example from diols, triols, tetraols and polyols having at least five hydroxyl groups.
• preferred components (A-1) are selected from compounds of the general formula (VIa),
• Preferred components (A-1) can also be selected from compounds of the general formula (Va),
• component (A-1) from aromatic compounds having two aromatic hydroxyl groups.
• Suitable aromatic compounds having two aromatic hydroxyl groups are for example hydroquinone, naphthalene diols, such as for instance 1,2-naphthalene diol, 2,6-naphthalene diol, 2,7-naphthalene diol, bis-(4-hydroxyphenyl), 2,2-bis-(4-hydroxyphenyl)propane, bis-(4-hydroxyphenyl)sulfide, bis-(4-hydroxyphenyl)ether, bis-(4-hydroxyphenyl)ketone, bis-(4-hydroxyphenyl)sulfone, bis-(4-hydroxyphenyl)methane, 1,1-bis-(4-hydroxyphenyl)cyclohexane, ⁇ , ⁇ ′-bis-(4-hydroxyphenyl)-p-diisopropylbenzene, 1,1-bis-(4-hydroxypheny
• Component (A-2) denotes polyethers having at least two terminal hydroxyl, carboxyl, amino or thiol groups, polyethers being preferred in particular that have at least two terminal hydroxyl groups.
• component (A-2) is selected from non-aromatic polyethers having at least two terminal hydroxyl, carboxyl, amino or thiol groups, non-aromatic polyethers having at least two terminal hydroxyl groups being particularly preferred.
• non-aromatic polyethers is understood to mean polyethers that comprise no aromatic structural element.
• Preferred components (A-2) are selected from compounds of the general formula (IX), P[—OH] m Formula (IX) in which m is a number from 2 to 100 and P denotes an m-valent polyalkylene oxide residue, such as for example an m-valent non-aromatic polyalkylene oxide residue.
• m is preferably a number from 2 to 50, particularly preferably from 2 to 10 and most particularly preferably from 2 to 4, wherein in particular m denotes 2.
• the m-valent polyalkylene oxide residue P can have a linear or branched structure.
• oligomeric or polymeric urethane group-free polyether compounds having a linear structure can be synthesized that exhibit good compatibility with the benzoxazine matrix.
• polyethers having more than two terminal hydroxyl groups as component (A-2), oligomeric or polymeric urethane group-free polyether compounds having a branched structure can be synthesized.
• Suitable components (A-2) can be selected for example from compounds of the general formula (VIIa),
• component (A-2) is selected from polyethers having at least two terminal hydroxyl, carboxyl, amino or thiol groups with a weight-average molecular weight (M w ) from 200 to 10,000 g/mol, preferably from 200 to 10,000 g/mol, preferably from 300 to 5000 g/mol and in particular from 500 to 2000 g/mol. It is furthermore advantageous for component (A-2) to be selected from the aforementioned polyethers, wherein these have a glass transition temperature (T g ) of less than 20° C., preferably less than 10° C. and particularly preferably less than 0° C.
• T g glass transition temperature
• Component (B-1) denotes polyethers having at least two terminal oxirane, aziridine or thiirane groups, polyethers being preferred in particular that have at least two terminal oxirane groups.
• component (B-1) is selected from non-aromatic polyethers having at least two terminal oxirane, aziridine or thiirane groups, non-aromatic polyethers having at least two terminal oxirane groups being particularly preferred.
• non-aromatic polyethers is defined as above.
• Component (B-1) is preferably selected from compounds of the general formula (X),
• each u′ in each repeating unit independently denotes a number from 1 to 10
• each residue R f and R g independently denotes a divalent group of compounds comprising 1 to 100 C atoms
• W is selected from —O—, —S— or —NH—
• each R in formula (X) and in each repeating unit is independently selected from hydrogen or linear or branched optionally substituted C 1-12 alkyl groups, R denoting hydrogen or methyl in particular.
• u in formula (X) denotes a number from 1 to 200, preferably a number from 3 to 5 and particularly preferably a number from 5 to 20 and/or u′ in formula (X) and in each repeating unit independently denotes 1, 2, 3, 4, 5, 6, 7 or 8, in particular 1 or 3.
• residues R f and R g in formula (X) are selected independently of each other from alkylene groups comprising 1 to 10 C atoms.
• residues R f and R g in formula (X) are selected independently of each other from linear alkylene groups comprising 1 to 6, in particular 1 or 2 carbon atoms, such as for example methylene and ethylene groups, R f and R g particularly preferably denoting a methylene group (—CH 2 —).
• Diglycidyl ethers of polyethers that are suitable as component (B-1) are available for example under the trade names DER-732, DER-736 (Dow Chemical Co.) or Adeka ED-506 (Adeka Corporation) or can be produced by the reaction of polyether polyols with epichlorohydrin known to the person skilled in the art.
• component (B-2) is selected from compounds of the general formula (VIIIa),
• R h in formula (VIIIa) and in each repeating unit is independently selected from alkylene groups comprising 1 to 10 C atoms and K in formula (VIIIa) and in each repeating unit independently denotes a divalent residue of aromatic dihydroxyl compounds following removal of both hydroxyl groups.
• r is a number from 0 to 2, in particular from 0 to 1, such as for example 0, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1.
• R h is selected in particular from linear alkylene groups comprising 1 to 6 carbon atoms, in particular 1 or 2 carbon atoms, such as for example methylene and ethylene groups, R f particularly preferably denoting a methylene group (—CH 2 —).
• Divalent residue K is formally obtained by removing two hydroxyl groups from aromatic dihydroxyl compounds and is as defined in formula (I).
• Diglycidyl ethers of bisphenol A or bisphenol F which are available for example under the trade names Epon 825, Epon 826, Epon 828, Epon 830, Epon 862, Epon 1001 (Hexion Specialty Chemicals Inc.) or DER-331, DER-332, DER-334 (Dow Chemical Co.) are suitable in particular as component (B-2).
• the aforementioned compounds can also be produced by reacting one or more suitable bisphenolic compounds with epichlorohydrin.
• Component (B-2) can furthermore be selected from compounds in which residue D in formula (VIII) comprises at least one aromatic group having at least one functional group of the following formula,
• R i denotes a divalent group of compounds comprising 1 to 100 C atoms and W is selected from —O—, —S— or —NH—.
• W denotes —O— and/or R i denotes an alkylene group having 1 to 10 C atoms, such as for example methylene or ethylene.
• Suitable residues D in formula (VIII) can be selected for example from the following aromatic residues,
• R i and W are as defined above and t is a number from 1 to 100,000, in particular from 1 to 10,000, particularly preferably from 1 to 1000.
• Corresponding components (B-2) are for example glycidyl ethers of phenolic resins, such as for example glycidyl ethers of novolak resins.
• the oligomeric or polymeric urethane group-free polyether compound is obtained by reacting at least one component (A-1) with at least one component (B-1) in the presence of at least one component (B-2).
• the oligomeric or polymeric urethane group-free polyether compounds obtained in this way have a greater effectiveness as impact modifiers than comparable products obtained by the exclusive reaction of at least one component (A-1) with at least one component (B-1).
• the molar ratio of the individual aforementioned components is preferably chosen in the reaction such that the oligomeric or polymeric urethane group-free polyether compound obtained has exclusively terminal oxirane, aziridine or thiirane groups, in particular exclusively terminal oxirane groups.
• At least one oligomeric or polymeric urethane group-free polyether compound is advantageous for at least one oligomeric or polymeric urethane group-free polyether compound to be obtained by reacting at least one component A with at least one component B, component A being selected from the group consisting of
• each residue R d and R e independently denotes a divalent group of compounds comprising 1 to 100 C atoms
• each residue X′ is independently selected from —O—, —S—, —NH— or a carboxyl group of the general form —(C ⁇ O)O—, in which the C atom of the carboxyl group is always connected to the residue D
• W is selected from —O—, —S— or —NH— and the residue D comprises at least one aromatic group, with the proviso that the exclusive reaction of one or more component(s) satisfying the definition of (A-1) with one or more component(s) satisfying the definition of (B-2) and the exclusive reaction of one or more component(s) satisfying the definition of (A-2) with one or more component(s) satisfying the definition of (B-1) is excluded.
• non-aromatic polyethers is understood to mean polyethers that comprise no aromatic structural element.
• the aforementioned oligomeric or polymeric urethane group-free polyether compound makes it possible to produce polymerizable compositions that in the cured state exhibit particularly good fracture-mechanical properties.
• j denotes a number from 0 to 4
• Q is selected from the group consisting of alkylene, oxygen, sulfur, sulfoxide, sulfone and a direct, covalent bond and each residue R c is independently selected from halogen, in particular fluorine, chlorine, bromine or iodine, C 1-40 alkyl, for instance methyl, ethyl, isopropyl, C 2-40 alkenyl, C 1-40 alkoxyl and C 7-13 aralkyl, with at least one component (B-1), selected from compounds of the general formula (Xa),
• each u′ in each repeating unit independently denotes a number from 1 to 10
• W and z are each independently selected from —O—, —S— or —NH—
• each R in formula (XIa) and in each repeating unit is independently selected from hydrogen or linear or branched optionally substituted C 1-12 alkyl groups, R denoting hydrogen or methyl in particular, in the presence of at least one component (B-2), component (B-2) being selected from compounds of the general formula (VIIIb),
• the molar ratio of component (A-1) to component B (B-1+B-2) is in particular between 1:1.01 and 1:1.6, preferably between 1:1.1 and 1:1.3.
• the polymerizable composition according to the invention can contain one or more of the oligomeric or polymeric urethane group-free polyether compounds described in amounts from 2 to 60 wt. %, preferably from 5 to 40 wt. % and extremely preferably from 10 to 30 wt. %, relative in each case to the total amount of the polymerizable composition.
• the polymerizable composition comprises only one or more benzoxazine compounds as the polymerizable resin component.
• the polymerizable composition additionally to contain further polymerizable resin components.
• Suitable compounds can be selected for example from the group of epoxy resins, polyurethane resins, polyester resins, polyamide resins or phenolic resins or from any mixtures thereof.
• an “epoxy resin” is understood to be a resin composition formed on the basis of epoxide compounds or epoxide-containing compounds. Within the meaning of the present invention all oligomeric or polymeric urethane group-free polyether compounds of the present invention are explicitly excluded from the designation “epoxy resin”, even if they contain terminal oxirane groups.
• the epoxide compounds or epoxide-containing compounds of the epoxy resin system of the polymerizable preparation can comprise both oligomeric and monomeric epoxide compounds and epoxides of the polymeric type and can be aliphatic, cycloaliphatic, aromatic or heterocyclic compounds.
• Suitable epoxy resins within the context of the present invention are for example preferably selected from epoxy resins of the bisphenol A type, epoxy resins of the bisphenol S type, epoxy resins of the bisphenol F type, epoxy resins of the phenol-novolak type, epoxy resins of the cresol-novolak type, epoxidized products of numerous dicyclopentadiene-modified phenolic resins, obtainable by reacting dicyclopentadiene with numerous phenols, epoxidized products of 2,2′,6,6′-tetramethylbisphenol, aromatic epoxy resins such as epoxy resins having a naphthalene framework and epoxy resins having a fluorene framework, aliphatic epoxy resins, alicyclic epoxy resins such as 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexane carboxylate and bis(3,4-epoxycyclohexyl)adipate and epoxy resins having at least one heterocyclic ring.
• the epoxy resins comprise in particular octadecylene oxide, styrene oxide, vinyl cyclohexene oxide, glycidol, vinyl cyclohexene dioxide, 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexene carboxylate, 3,4-epoxy-6-methylcyclohexylmethyl-3,4-epoxy-6-methylcyclohexene carboxylate, bis(3,4-epoxy-6-methylcyclohexylmethyl)adipate, bis(2,3-epoxycyclopentyl)ether, aliphatic dipentene dioxide, epoxidized polybutadiene (e.g.
• Particularly preferred epoxy resins within the meaning of the present invention are cycloaliphatic epoxy resins that are available commercially for example under the trade name CY179 (Huntsman), ACHWL CER 4221 (Achiewell, LLC) or Cyracure 6105/6110 (DOW Chemical).
• the polymerizable preparation according to the invention comprises a mixture of a plurality of the aforementioned epoxy resins.
• the proportion of the epoxy resin or of the mixture of a plurality of epoxy resins relative to the total amount of the polymerizable preparation is preferably 5 to 50 wt. %, particularly preferably 10 to 30 wt. % and extremely preferably 15 to 25 wt. %.
• compositions according to the invention generally also contain additives, such as for example ground or precipitated chalks, carbon black, calcium magnesium carbonates, barytes, and in particular silica fillers of the aluminum magnesium calcium silicate type, for example wollastonite or chlorite.
• additives such as for example ground or precipitated chalks, carbon black, calcium magnesium carbonates, barytes, and in particular silica fillers of the aluminum magnesium calcium silicate type, for example wollastonite or chlorite.
• compositions according to the invention can furthermore contain other additives such as for example plasticizers, reactive thinners, further impact modifiers, rheology aids, wetting agents, antioxidants, stabilizers and/or colored pigments.
• additives such as for example plasticizers, reactive thinners, further impact modifiers, rheology aids, wetting agents, antioxidants, stabilizers and/or colored pigments.
• the compositions are however preferably free from plasticizers.
• compositions according to the invention comprise, relative to the total amount of the polymerizable composition:
• the present invention also provides the polymerization product of the polymerizable composition according to the invention.
• the critical stress intensity factor K1c and the critical energy release rate G1c can be determined in accordance with ASTM D5045-96 using the single etch notch bending method (SENB), wherein in each case a specimen of dimensions 56 mm ⁇ 12.7 mm ⁇ 3.2 mm can be used.
• Polymerization of the polymerizable benzoxazine compound or the mixture of various polymerizable benzoxazine compounds can take place at elevated temperature by means of a self-initiating mechanism (thermal polymerization) or by addition of cationic initiators.
• Suitable cationic initiators are for example Lewis acids or other cationic initiators, such as for example metal halides, organometallic reagents, such as metalloporphyrins, methyl tosylates, methyl triflates or trifluorosulfonic acids.
• Basic reagents can likewise be used to initiate polymerization of the polymerizable benzoxazine compound or the mixture of various polymerizable benzoxazine compounds.
• Suitable basic reagents can be selected for example from imidazole or imidazole derivatives.
• Thermal polymerization of the polymerizable composition according to the invention preferably takes place at temperatures from 150 to 300° C., in particular at temperatures from 160 to 220° C. Through the use of the aforementioned initiators and/or other reagents the polymerization temperature can also be lower.
• the polymerization product according to the invention incorporates a layer or a bundle of fibers, wherein the fibers are treated prior to curing (polymerization) with the polymerizable composition according to the invention.
• the subsequent curing results in a fiber-reinforced composite material.
• the present invention therefore also provides a method for producing a polymerization product of the polymerizable composition according to the invention, wherein the cited composition incorporates a layer or a bundle of fibers and the fibers are treated prior to curing with the polymerizable composition according to the invention.
• the method according to the invention comprises the following steps:
• elevated temperature is understood to mean in particular temperatures from 40° C. to 300° C., preferably from 50° C. to 280° C. and particularly preferably from 80° C. to 250° C.
• the cited fibers are preferably selected from glass fibers, carbon fibers, aramid fibers, boron fibers, aluminum oxide fibers, silicon carbide fibers. Two or more of these fibers can be used as a mixture.
• the use of carbon fibers is particularly preferred in order to produce a product that is relatively low in weight and has a relatively long lifetime.
• the layer or bundle of fibers is not tied to a defined form or alignment and so for example long fibers laid parallel to one another in one direction, tow yarns, woven fabric (cloth), mats, knitted fabric or lace can be used.
• the composite systems in the form of fiber-reinforced composite materials produced by the cited method according to the invention can be used for example in aircraft construction or in the automotive industry.
• prepregs or towpregs made from fibers (reinforcing fibers) and uncured polymerizable compositions are produced as an intermediate, which can then be manually laminated and heat-cured.
• a liquid, heat-curable polymerizable composition is injected into a reinforcing fiber substrate located in a mold and this is then heat-cured in order to obtain a fiber-reinforced composite material.
• VaRTM vacuum-assisted resin transfer molding
• the present invention also provides an adhesive, sealant or coating agent comprising the polymerizable composition according to the invention.
• the present invention likewise provides the use of one or more of the aforementioned oligomeric or polymeric urethane group-free polyether compounds as impact modifiers for a polymerization product containing at least one polymerizable benzoxazine compound in polymerized form.
• Araldite MY 0510 (p-Aminophenol) triglycidyl ether, Huntsman
• a mixture consisting of bisphenol A (component A-1) and DER 732 or DER 736 (component B-1) was placed in a reaction vessel.
• DER 331 component B-2
• tetrabutyl ammonium bromide 0.3 wt. %
• oligomeric or polymeric urethane group-free polyether compounds produced by the procedure described above are shown in Table 1 with details of the molar ratios of the individual components in the production of the cited polyether compounds.
• the polymerizable composition was produced in a 500-ml reaction flask. 120 g of the benzoxazine compound (Box) shown above and 40 g of the cycloaliphatic epoxy resin CER 4221 (Achiewell) were placed in this flask. The corresponding amount of the oligomeric or polymeric urethane group-free polyether compounds and optionally a curing catalyst (diethylamine salt of trifluoromethane sulfonic acid, Nacure Super A233, King Industries) was added while stirring.
• a curing catalyst diethylamine salt of trifluoromethane sulfonic acid, Nacure Super A233, King Industries
• the mixture was homogenized under vacuum ( ⁇ 10 mbar) at 80° C. while stirring for 15 to 30 minutes and then stored in closed containers.
• Table 2 shows the proportions of the individual constituents in the polymerizable compositions, relative in each case to the total amount of the polymerizable composition.
• compositions Polyether Nacure CER compound Super Polymerizable Box 4221 or reference A233 composition [wt. %] [wt. %] compound [wt. %] a 1 (ref.) 80 20 — — 2 (ref.) 80 20 — 1 2a (ref.) 60 20 #16, 20 wt. % 1 3 60 20 #1, 20 wt. % — 4 60 20 #2, 20 wt. % — 5 60 20 #3, 20 wt. % — 6 60 20 #4, 20 wt. % — 7 60 20 #5, 20 wt. % — 8 60 20 #13, 20 wt. % 1 9 60 20 #6, 20 wt.
• the wt. % FIGURE for Nacure Super A233 is relative to the total amount of resin components (Box + CER 4221 + polyether compound)
• the polymerizable compositions were thermally cured in an autoclave at 180° C. within 90 min.
• the cured specimens (polymerization products) were then cooled to room temperature and characterized by means of the following analytical methods.
• the critical stress intensity factor K1c and the G1c value were determined in accordance with ASTM D5045-96 using the single etch notch bending method (SENB), wherein in each case a specimen of dimensions 56 mm ⁇ 12.7 mm ⁇ 3.2 mm was used.
• SENB single etch notch bending method
• Table 3 shows that the polymerization products according to the invention have very high K1c and G1c values and a high flexural modulus.
• the mechanical data shown thus demonstrates that the oligomeric or polymeric urethane group-free polyether compounds of the present invention are outstandingly suitable as impact modifiers for benzoxazine-based resin systems.

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